Canonical Allele Identifier: PA2826625086
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 2101336
ClinVar RCV Id: RCV003016854

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Glu158Asp
CA346740607
NM_001281492.2:c.474A>C
CA346740608
NM_001281492.2:c.474A>T